training update: preventive controls regulator training · overview/topics • course description...
TRANSCRIPT
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Training Update: Preventive Controls Regulator Training
Patricia L. AlcockDirector, Office of Training, Education and
DevelopmentFood and Drug Administration
1/30/20189:00 AM
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Today’s Agenda
- Preventive Controls for Human Food Training
- Future Training Considerations
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Preventive Controls for Human Food Regulators Training Course
FD254
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OVERVIEW/TOPICS
• Course Description• Course Goal/Objectives• Course Outline• Class Schedule for FY18
Reference: PC CAP Webinar, 12/13/2017
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FD254 Course Description
• Learn how to apply a systematic approach to inspect food manufacturing firms based on the Current GMP, Hazard Analysis and Risk-Based Preventive Control Regulation, and to document violations of this regulation observed during the inspection.
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FD254 Course Description
• Introduces Current GMP, Hazard Analysis and Risk-Based Preventive Controls (GMP/PC).
• GMP/PC provides an overview of the regulatory requirements for food facilities and how to apply them during an inspection.
• Participants complete mock scenarios perform a final assessment to reinforce their understanding through application of the course material.
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FD254 Objectives
1. Describe the guiding principles for systems-based inspection process.
2. Interpret 21 CFR 117.3. Determine the scope of the inspection by asking
open-ended questions to verify establishment type and to identify product for coverage.
4. Gather information for hazard analysis through interview and observation.
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FD254 Objectives
5. Conduct a hazard analysis based on information gathered.
6. Evaluate components of the food safety plan for adequacy.
7. Using observation skills and interviewing techniques, formulate open-ended questions to determine if a facility is implementing their food safety plan.
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FD254 Objectives
8. Provide the basis for reporting observation of non-compliance of the preventive controls for human foods regulation.
9. Review a firm’s Food Safety Plan to determine compliance with the PC rule.
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FD254 Course Prerequisites
• ORA’s New Hire Investigator Training Program or equivalent
• Level 1 Investigator Certification or equivalent (ORA Staff)
• Successfully Completed FD180 (OR both FD150 & FD151) • Watch FD8000 webinar on Modernized GMPs (live or
recorded)(available via ORA OTED LMS)
• Successfully Complete FSPCA Human Food Training• Successfully Complete the FD254W100 online course
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Introduction to PC for Human Foods Web CourseFD254W100*
Online Module 1: Course OverviewOnline Module 2: Modernized Good Manufacturing Practices (GMPs)Online Module 3: Modernized Good Manufacturing Practices (GMPs)Online Module 4: Subparts D&E Modified Requirements & Withdrawal of
Qualified Facility ExemptionOnline Module 5: Subpart F: Requirements Applying to Records That Must
be Established & MaintainedOnline Module 6: Subpart G Supply-Chain ProgramOnline Module 7: Training Requirements Online Module 8: Microbiological Controls for LACF & Acidified Foods
*Must be completed before take FD254
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FD254 Classroom Course Outline
• Introduction: Systems Thinking• Module 1: Intro to 21 CFR 117• Module 2: Initial Interview• Module 3: Gathering Information for your
Hazard Analysis
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FD254 Classroom Course Outline
• Module 4: Modified Requirements & Withdrawal of Qualified Facility Exemption
• Module 5: Requirements Applying to Records That Must be Established and Maintained
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FD254 Classroom Course Outline
• Module 6: Evaluating the Adequacy of the Food Safety Plan
• Module 7: Assess Food Safety Plan Implementation
• Module 8: Document Inspection Observations
• Final Assessment: Application of all Modules
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FD254 FY18 Course Schedule
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FY18 CLASS SCHEDULE
• States will receive at minimum 40% courseslots.
• OTED/OP has prioritized attendance of those states already committed to complete the work.
• OTED/OP followed established procedure for slot allocations amongst the remaining state in collaboration with ORA’s Office of Partnership and the Pre-Registration Workbook.
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FY19 CLASS SCHEDULE
• Need to understand the needs of States andtheir inspection staff.
• AFDO Data call will be used to helpdetermine number of needed slots per FY19and FY20.
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Future Training Considerations
• Training WG on Alternative Options – Develop proposals to address:
• Equivalency Tools– Training Course– Individuals
• FDA Course Training Hand Off– Same course content– Qualified Instructors
• Train the Trainer Programs
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Future Training Considerations
• Training WG on Alternative Options– Next Steps?
• Develop and finalize recommendations• ORA & FDA Review recommendations • Socialize recommendations
– PFP, CFP, AFDO, AAFCO, NASDA
• Determine interest by State Ag and Health • Impact of scaling up pilot programs • Develop Implementation and Communication Plan
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Future Training Considerations
• Train the Trainer Programs– Interest by States?– Availability of State personnel?– Process/Procedures– Requirements for Consistency
Where can AFDO or MFRP Alliance assist?
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Future Training Considerations
• FDA/ORA Training Needs Survey– FY19 & Beyond
• MFRPA & One time funding for FD152– Collaboration with academia
• IFSS National Curriculum Standard
Where can AFDO or MFRP Alliance assist?
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Contact Information
Patricia L. Alcock
Director, Office of Training, Education and Development
FDA/Office of Regulatory Affairs
Email: [email protected]